Canonical Allele Identifier: CA2639075589

Gene: RPS6KB1

Linked Data

• gnomAD v4: 17-59946918-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.59946918A>G , CM000679.2:g.59946918A>G	GRCh38
NC_000017.10:g.58024279A>G , CM000679.1:g.58024279A>G	GRCh37
NC_000017.9:g.55379061A>G	NCBI36
NG_029513.1:g.58837A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225577.9:c.*130A>G MANE Select	ENSP00000225577.4:n.*130A>G
ENST00000225577.8:c.*130A>G	ENSP00000225577.4:n.*130A>G
ENST00000393021.7:c.*130A>G	ENSP00000376744.3:n.*130A>G
ENST00000406116.7:c.1341-669A>G	ENSP00000384335.3:n.1341-669A>G
ENST00000443572.6:c.*130A>G	ENSP00000441993.1:n.*130A>G
ENST00000472940.5:c.*1743A>G	ENSP00000468058.1:n.*1743A>G
ENST00000475155.1:n.696A>G
ENST00000591035.1:c.149+1400A>G	ENSP00000468280.1:n.149+1400A>G
NM_001272042.1:c.*130A>G	NP_001258971.1:n.*130A>G
NM_001272043.1:c.1341-669A>G	NP_001258972.1:n.1341-669A>G
NM_001272044.1:c.*130A>G	NP_001258973.1:n.*130A>G
NM_001272060.1:c.*130A>G	NP_001258989.1:n.*130A>G
NM_003161.3:c.*130A>G	NP_003152.1:n.*130A>G
XM_011525101.1:c.*130A>G	XP_011523403.1:n.*130A>G
XM_011525103.1:c.*130A>G	XP_011523405.1:n.*130A>G
XM_011525104.1:c.*130A>G	XP_011523406.1:n.*130A>G
XM_011525101.3:c.*130A>G	XP_011523403.1:n.*130A>G
XM_011525103.3:c.*130A>G	XP_011523405.1:n.*130A>G
XM_017024929.1:c.*130A>G	XP_016880418.1:n.*130A>G
XM_017024930.2:c.*130A>G	XP_016880419.1:n.*130A>G
XM_017024931.2:c.*130A>G	XP_016880420.1:n.*130A>G
XM_017024932.2:c.*130A>G	XP_016880421.1:n.*130A>G
XM_017024933.2:c.*130A>G	XP_016880422.1:n.*130A>G
XR_001752581.2:n.1954A>G
XR_001752582.2:n.1761A>G
XR_001752583.2:n.1653A>G
XR_002958051.1:n.3445A>G
NM_003161.4:c.*130A>G MANE Select	NP_003152.1:n.*130A>G
NM_001272043.2:c.1341-669A>G	NP_001258972.1:n.1341-669A>G
NM_001369669.1:c.*130A>G	NP_001356598.1:n.*130A>G
NM_001369670.1:c.*130A>G	NP_001356599.1:n.*130A>G
NM_001369671.1:c.*130A>G	NP_001356600.1:n.*130A>G
NM_001369672.1:c.*130A>G	NP_001356601.1:n.*130A>G
NM_001369673.1:c.*1159A>G	NP_001356602.1:n.*1159A>G
NM_001369674.1:c.*1301A>G	NP_001356603.1:n.*1301A>G
NM_001369675.1:c.*1193A>G	NP_001356604.1:n.*1193A>G
NM_001369676.1:c.*1062A>G	NP_001356605.1:n.*1062A>G
NM_001369677.1:c.*1412A>G	NP_001356606.1:n.*1412A>G
NM_001369678.1:c.*1159A>G	NP_001356607.1:n.*1159A>G
NM_001369679.1:c.*1416A>G	NP_001356608.1:n.*1416A>G
NR_161455.1:n.1624A>G
NR_161456.1:n.1775A>G
NR_161457.1:n.1671A>G
NR_161458.1:n.1969A>G
NR_161459.1:n.1750A>G
NR_161460.1:n.2015A>G
NR_161461.1:n.1776A>G
NR_161462.1:n.1668A>G
NM_001272042.2:c.*130A>G	NP_001258971.1:n.*130A>G
NM_001272044.2:c.*130A>G	NP_001258973.1:n.*130A>G
NM_001272060.2:c.*130A>G	NP_001258989.1:n.*130A>G